ClinVar Miner

List of variants in gene SCN10A reported as uncertain significance for not provided

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Total variants: 45
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HGVS dbSNP
NM_006514.3(SCN10A):c.1004A>G (p.Asn335Ser) rs966272776
NM_006514.3(SCN10A):c.1110G>T (p.Gly370=) rs267599808
NM_006514.3(SCN10A):c.1715C>T (p.Pro572Leu) rs553784643
NM_006514.3(SCN10A):c.1754C>T (p.Ser585Leu) rs781705809
NM_006514.3(SCN10A):c.1788G>T (p.Leu596Phe) rs764965507
NM_006514.3(SCN10A):c.1858G>A (p.Val620Ile) rs151303346
NM_006514.3(SCN10A):c.1942T>A (p.Cys648Ser) rs1553619038
NM_006514.3(SCN10A):c.2026G>A (p.Val676Met) rs576503650
NM_006514.3(SCN10A):c.2062G>A (p.Gly688Ser) rs779931477
NM_006514.3(SCN10A):c.232C>T (p.Pro78Ser) rs753292241
NM_006514.3(SCN10A):c.2367C>A (p.Asn789Lys) rs770046573
NM_006514.3(SCN10A):c.2427del (p.Glu811fs) rs751810656
NM_006514.3(SCN10A):c.2428G>T (p.Gly810Trp) rs145712124
NM_006514.3(SCN10A):c.2431G>C (p.Glu811Gln) rs77049337
NM_006514.3(SCN10A):c.243T>A (p.Asp81Glu) rs1060501717
NM_006514.3(SCN10A):c.2441G>A (p.Arg814His) rs139861061
NM_006514.3(SCN10A):c.2554G>A (p.Glu852Lys) rs375274122
NM_006514.3(SCN10A):c.2593A>G (p.Ile865Val) rs1553617020
NM_006514.3(SCN10A):c.322C>T (p.Arg108Trp) rs1131691525
NM_006514.3(SCN10A):c.365C>T (p.Thr122Met) rs142884499
NM_006514.3(SCN10A):c.3704C>T (p.Ala1235Val) rs765984332
NM_006514.3(SCN10A):c.3712C>G (p.Leu1238Val) rs960602539
NM_006514.3(SCN10A):c.3859G>A (p.Val1287Ile) rs145032037
NM_006514.3(SCN10A):c.3908T>C (p.Phe1303Ser) rs1064796846
NM_006514.3(SCN10A):c.4028G>A (p.Trp1343Ter) rs756036768
NM_006514.3(SCN10A):c.4118T>G (p.Met1373Arg) rs1131691400
NM_006514.3(SCN10A):c.4164G>A (p.Trp1388Ter) rs756253735
NM_006514.3(SCN10A):c.4639G>T (p.Val1547Leu) rs377492327
NM_006514.3(SCN10A):c.470+8G>A rs1064797293
NM_006514.3(SCN10A):c.4724T>C (p.Ile1575Thr) rs1064796379
NM_006514.3(SCN10A):c.4762C>T (p.Arg1588Ter) rs142537392
NM_006514.3(SCN10A):c.4763G>A (p.Arg1588Gln) rs376439863
NM_006514.3(SCN10A):c.4915G>A (p.Asp1639Asn) rs368582725
NM_006514.3(SCN10A):c.495del (p.Phe166fs) rs1553623239
NM_006514.3(SCN10A):c.4985_4986del (p.Gly1662fs) rs1553613042
NM_006514.3(SCN10A):c.5243G>C (p.Trp1748Ser) rs1064797008
NM_006514.3(SCN10A):c.5351T>C (p.Ile1784Thr) rs1085307543
NM_006514.3(SCN10A):c.5539C>T (p.Arg1847Ter) rs199503439
NM_006514.3(SCN10A):c.5548C>T (p.Gln1850Ter) rs149504103
NM_006514.3(SCN10A):c.55G>A (p.Glu19Lys) rs141810266
NM_006514.3(SCN10A):c.5626A>G (p.Thr1876Ala) rs759136534
NM_006514.3(SCN10A):c.5693C>T (p.Thr1898Ile) rs1553612806
NM_006514.3(SCN10A):c.621T>A (p.Asp207Glu) rs377716847
NM_006514.3(SCN10A):c.724T>A (p.Ser242Thr) rs140288103
NM_006514.3(SCN10A):c.905G>A (p.Arg302Gln) rs201955990

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